Barely Significant
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Folate Pathway Gene Single Nucleotide Polymorphisms and Neural Tube Defects: A Systematic Review and Meta-Analysis.

J Pers Med · 2022 · PMC9605131 · PMID 36294748

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highly significantno p-value reported
[ 87 ], both case (genotype and allele frequencies) and maternal (allele frequencies only) groups have highly significant associations between NTD risk and the MTHFD1 SNP G1958A (R653Q).

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